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    Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations von Rebbeck, Timothy R., Hamann, Ute, Olah, Edith, Solano, Angela R., Teo, Soo‐Hwang, Chan, TL, Couch, Fergus J., Palmero, Edenir Inêz, Park, Sue Kyung, Parsons, Michael T., Leslie, Goska, Aalfs, Cora M., Adlard, Julian, Agata, Simona, Aittomäki, Kristiina, Andrulis, Irene L., Barkardottir, Rosa B., Benitez, Javier, Blanco, Amie M., Bonadona, Valérie, Bonanni, Bernardo, Caligo, Maria A., Campbell, Ian, Chung, Wendy K., Claes, Kathleen B.M., Cook, Jackie, Davidson, Rosemarie, Leeneer, Kim, Domchek, Susan M., Dorfling, Cecilia M., Velazquez, Carolina, Easton, Douglas F., Feliubadaló, Lidia, Ferrer, Sandra Fert, Foretova, Lenka, Galvão, Henrique C. R., Garber, Judy, Gesta, Paul, Giannini, Giuseppe, Gutierrez‐Barrera, Angelica, Hogervorst, Frans B.L., Imyanitov, Evgeny N., Izquierdo, Angel, Jakubowska, Anna, James, Paul, Janavicius, Ramunas, John, Esther M., Vijai, Joseph, Karlan, Beth Y., Kast, Karin, Investigators, KConFab, Korach, Jacob, Laitman, Yael, Lasset, Christine, Lázaro, Conxi, Lee, Annette, Lee, Min Hyuk, Lester, Jenny, Liljegren, Annelie, Machackova, Eva, Mari, Véronique, Meijers‐Heijboer, Hanne E.J., Miller, Austin, Montagna, Marco, Mulligan, Anna Marie, Ngeow, Joanne, Nielsen, Henriette Roed, Nussbaum, Robert L., Offit, Kenneth, Öfverholm, Anna, Osorio, Ana, Papp, Janos, Pedersen, Inge Sokilde, Peruga, Nina, Peterlongo, Paolo, Radice, Paolo, Robson, Mark, Rodriguez, Gustavo C., Rudaitis, Vilius, Schmidt, Ane Y., Senter, Leigha, Singer, Christian F., Skytte, Anne‐Bine, Sobol, Hagay, Teixeira, Manuel R., Tischkowitz, Marc, Toland, Amanda Ewart, Topka, Sabine, Trainer, Alison H, Varesco, Liliana, Varon‐Mateeva, Raymonda, Vega, Ana, Wachenfeldt, Anna, Wang‐Gohrke, Shan, Weber, Bernhard H. F., Yannoukakos, Drakoulis, Zorn, Kristin K., Chenevix‐Trench, Georgia, Spurdle, Amanda B., Nathanson, Katherine L.

    Veröffentlicht in Human mutation

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    Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations von Hamann, Ute, Huo, Dezheng, Solano, Angela R, Weitzel, Jeffrey N, Chan, TL, Goldgar, David E, van Rensburg, Elizabeth J, McGuffog, Lesley, Agata, Simona, Azzollini, Jacopo, Balmaña, Judith, Barile, Monica, Barrowdale, Daniel, Blanco, Amie M, Blazer, Kathleen R, Blok, Marinus J, Brewer, Carole, Buecher, Bruno, Caputo, Sandrine M, Chung, Wendy K, de la Hoya, Miguel, de Pauw, Antoine, Diez, Orland, Dworniczak, Bernd, Ehrencrona, Hans, EMBRACE, Evans, D Gareth, Faivre, Laurence, Gauthier-Villars, Marion, GEMO Study Collaborators, Gesta, Paul, Giraud, Sophie, Glendon, Gord, Gutierrez-Barrera, Angelica, HEBON, Henderson, Alex, Hentschel, Julia, Hogervorst, Frans BL, James, Paul, John, Esther M, Kaczmarek, Katarzyna, Karlan, Beth Y, Investigators, KConFab, Konstantopoulou, Irene, Korach, Jacob, Laitman, Yael, Lasset, Christine, Lesueur, Fabienne, Liljegren, Annelie, Lu, Karen H, Mari, Véronique, Martínez-Bouzas, Cristina, Meijers-Heijboer, Hanne EJ, Meindl, Alfons, Montagna, Marco, Nevanlinna, Heli, Nielsen, Finn Cilius, Öfverholm, Anna, Ong, Kai-Ren, Papp, Janos, Pedersen, Inge Sokilde, Pohl, Esther, Pradhan, Nisha, Prajzendanc, Karolina, Prieur, Fabienne, Radice, Paolo, Rantala, Johanna, Rashid, Muhammad Usman, Rhiem, Kerstin, Robson, Mark, Rodriguez, Gustavo C, Rogers, Mark T, Schmidt, Ane Y, Shah, Payal D, Sharma, Priyanka, Simard, Jacques, Singer, Christian F, Skytte, Anne-Bine, Slavin, Thomas P, Steele, Linda, Sukiennicki, Grzegorz, Tan, Yen Y, Teixeira, Manuel R, Tognazzo, Silvia, Trainer, Alison H, Tung, Nadine, van Asperen, Christi J, van der Kolk, Lizet E, van der Luijt, Rob B, Van Heetvelde, Mattias, Varesco, Liliana, Villarreal-Garza, Cynthia, Walker, Lisa, Wang-Gohrke, Shan, Yoon, Sook-Yee, Zanzottera, Cristina, Zorn, Kristin K, Hutten Selkirk, Christina G, Hulick, Peter J, Nathanson, Katherine L

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